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Published in 2019 at "Human molecular genetics"
DOI: 10.1093/hmg/ddz221
Abstract: UBE3A encodes a E3 ubiquitin ligase whose loss from the maternal allele causes the neurodevelopmental disorder Angelman syndrome. Previous studies of UBE3A function have not examined full Ube3a deletion in mouse, the complexity of imprinted…
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Keywords:
wnt signaling;
gene networks;
ube3a loss;
ube3a deletion ... See more keywords